182 related articles for article (PubMed ID: 12417412)
1. Mice with a homozygous deletion of the Mgat2 gene encoding UDP-N-acetylglucosamine:alpha-6-D-mannoside beta1,2-N-acetylglucosaminyltransferase II: a model for congenital disorder of glycosylation type IIa.
Wang Y; Schachter H; Marth JD
Biochim Biophys Acta; 2002 Dec; 1573(3):301-11. PubMed ID: 12417412
[TBL] [Abstract][Full Text] [Related]
2. Modeling human congenital disorder of glycosylation type IIa in the mouse: conservation of asparagine-linked glycan-dependent functions in mammalian physiology and insights into disease pathogenesis.
Wang Y; Tan J; Sutton-Smith M; Ditto D; Panico M; Campbell RM; Varki NM; Long JM; Jaeken J; Levinson SR; Wynshaw-Boris A; Morris HR; Le D; Dell A; Schachter H; Marth JD
Glycobiology; 2001 Dec; 11(12):1051-70. PubMed ID: 11805078
[TBL] [Abstract][Full Text] [Related]
3. Immune dysfunction in MGAT2-CDG: A clinical report and review of the literature.
Poskanzer SA; Schultz MJ; Turgeon CT; Vidal-Folch N; Liedtke K; Oglesbee D; Gavrilov DK; Tortorelli S; Matern D; Rinaldo P; Bennett JT; Thies JM; Chang IJ; Beck AE; Raymond K; Allenspach EJ; Lam C
Am J Med Genet A; 2021 Jan; 185(1):213-218. PubMed ID: 33044030
[TBL] [Abstract][Full Text] [Related]
4. The role of the GlcNAc(beta)1,2Man(alpha)- moiety in mammalian development. Null mutations of the genes encoding UDP-N-acetylglucosamine:alpha-3-D-mannoside beta-1,2-N-acetylglucosaminyltransferase I and UDP-N-acetylglucosamine:alpha-D-mannoside beta-1,2-N-acetylglucosaminyltransferase I.2 cause embryonic lethality and congenital muscular dystrophy in mice and men, respectively.
Schachter H
Biochim Biophys Acta; 2002 Dec; 1573(3):292-300. PubMed ID: 12417411
[TBL] [Abstract][Full Text] [Related]
5. Carbohydrate-deficient glycoprotein syndrome type II.
Schachter H; Jaeken J
Biochim Biophys Acta; 1999 Oct; 1455(2-3):179-92. PubMed ID: 10571011
[TBL] [Abstract][Full Text] [Related]
6. Mutations in the MGAT2 gene controlling complex N-glycan synthesis cause carbohydrate-deficient glycoprotein syndrome type II, an autosomal recessive disease with defective brain development.
Tan J; Dunn J; Jaeken J; Schachter H
Am J Hum Genet; 1996 Oct; 59(4):810-7. PubMed ID: 8808595
[TBL] [Abstract][Full Text] [Related]
7. The human UDP-N-acetylglucosamine: alpha-6-D-mannoside-beta-1,2- N-acetylglucosaminyltransferase II gene (MGAT2). Cloning of genomic DNA, localization to chromosome 14q21, expression in insect cells and purification of the recombinant protein.
Tan J; D'Agostaro AF; Bendiak B; Reck F; Sarkar M; Squire JA; Leong P; Schachter H
Eur J Biochem; 1995 Jul; 231(2):317-28. PubMed ID: 7635144
[TBL] [Abstract][Full Text] [Related]
8. UDP-N-acetylglucosamine:alpha-3-D-mannoside beta-1,2-N-acetylglucosaminyltransferase I and UDP-N-acetylglucosamine:alpha-6-D-mannoside beta-1,2-N-acetylglucosaminyltransferase II in Caenorhabditis elegans.
Chen S; Tan J; Reinhold VN; Spence AM; Schachter H
Biochim Biophys Acta; 2002 Dec; 1573(3):271-9. PubMed ID: 12417409
[TBL] [Abstract][Full Text] [Related]
9. Isolation, characterization and inactivation of the mouse Mgat3 gene: the bisecting N-acetylglucosamine in asparagine-linked oligosaccharides appears dispensable for viability and reproduction.
Priatel JJ; Sarkar M; Schachter H; Marth JD
Glycobiology; 1997 Feb; 7(1):45-56. PubMed ID: 9061364
[TBL] [Abstract][Full Text] [Related]
10. UDP-N-acetylglucosamine:alpha-6-D-mannoside beta1,6 N-acetylglucosaminyltransferase V (Mgat5) deficient mice.
Dennis JW; Pawling J; Cheung P; Partridge E; Demetriou M
Biochim Biophys Acta; 2002 Dec; 1573(3):414-22. PubMed ID: 12417426
[TBL] [Abstract][Full Text] [Related]
11. Cloning and expression of a novel UDP-GlcNAc:alpha-D-mannoside beta1,2-N-acetylglucosaminyltransferase homologous to UDP-GlcNAc:alpha-3-D-mannoside beta1,2-N-acetylglucosaminyltransferase I.
Zhang W; Betel D; Schachter H
Biochem J; 2002 Jan; 361(Pt 1):153-62. PubMed ID: 11742540
[TBL] [Abstract][Full Text] [Related]
12. Congenital disorders of glycosylation type Ia and IIa are associated with different primary haemostatic complications.
Van Geet C; Jaeken J; Freson K; Lenaerts T; Arnout J; Vermylen J; Hoylaerts MF
J Inherit Metab Dis; 2001 Aug; 24(4):477-92. PubMed ID: 11596651
[TBL] [Abstract][Full Text] [Related]
13. Human
Kadirvelraj R; Yang JY; Sanders JH; Liu L; Ramiah A; Prabhakar PK; Boons GJ; Wood ZA; Moremen KW
Proc Natl Acad Sci U S A; 2018 May; 115(18):4637-4642. PubMed ID: 29666272
[TBL] [Abstract][Full Text] [Related]
14. Transcriptional regulation of the human UDP-GlcNAc:alpha-6-D-mannoside beta-1-2-N-acetylglucosaminyltransferase II gene (MGAT2) which controls complex N-glycan synthesis.
Chen SH; Zhou S; Tan J; Schachter H
Glycoconj J; 1998 Mar; 15(3):301-8. PubMed ID: 9579808
[TBL] [Abstract][Full Text] [Related]
15. Congenital disorder of glycosylation type Ij (CDG-Ij, DPAGT1-CDG): extending the clinical and molecular spectrum of a rare disease.
Würde AE; Reunert J; Rust S; Hertzberg C; Haverkämper S; Nürnberg G; Nürnberg P; Lehle L; Rossi R; Marquardt T
Mol Genet Metab; 2012 Apr; 105(4):634-41. PubMed ID: 22304930
[TBL] [Abstract][Full Text] [Related]
16. N-glycan branching requirement in neuronal and postnatal viability.
Ye Z; Marth JD
Glycobiology; 2004 Jun; 14(6):547-58. PubMed ID: 15044398
[TBL] [Abstract][Full Text] [Related]
17. Functional roles of the bisecting GlcNAc in integrin-mediated cell adhesion.
Isaji T; Kariya Y; Xu Q; Fukuda T; Taniguchi N; Gu J
Methods Enzymol; 2010; 480():445-59. PubMed ID: 20816221
[TBL] [Abstract][Full Text] [Related]
18. Congenital disorders of glycosylation: The Saudi experience.
Alsubhi S; Alhashem A; Faqeih E; Alfadhel M; Alfaifi A; Altuwaijri W; Alsahli S; Aldhalaan H; Alkuraya FS; Hundallah K; Mahmoud A; Alasmari A; Mutairi FA; Abduraouf H; AlRasheed L; Alshahwan S; Tabarki B
Am J Med Genet A; 2017 Oct; 173(10):2614-2621. PubMed ID: 28742265
[TBL] [Abstract][Full Text] [Related]
19. Golgi N-glycan branching N-acetylglucosaminyltransferases I, V and VI promote nutrient uptake and metabolism.
Abdel Rahman AM; Ryczko M; Nakano M; Pawling J; Rodrigues T; Johswich A; Taniguchi N; Dennis JW
Glycobiology; 2015 Feb; 25(2):225-40. PubMed ID: 25395405
[TBL] [Abstract][Full Text] [Related]
20. Mgat2 ablation in the myeloid lineage leads to defective glycoantigen T cell responses.
Ryan SO; Leal SM; Abbott DW; Pearlman E; Cobb BA
Glycobiology; 2014 Mar; 24(3):262-71. PubMed ID: 24310166
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
